Senior Process Engineer - Pharma/Biotech Automation Expert

ENGAGE GROUP PTE. LTD.; Singapore; Sur place; SGD 120 000 - 210 000; Plein temps

Résumé du poste

ENGAGE GROUP PTE. LTD. in Singapore is seeking a Senior Process Engineer to lead process design in pharmaceutical and biotech manufacturing, bridging process engineering with automation to deliver GMP-compliant facilities.

You will work across concept through commissioning, collaborating with multidisciplinary teams, and applying knowledge of industry standards to optimise validation and CQV activities.

Qualifications

• Degree in Chemical Engineering, Process Engineering, Biotechnology, Automation Engineering, Mechatronics or related discipline.
• 5–10 years of relevant industry experience.
• Experience in pharmaceutical or biotech manufacturing, biologics or vaccine production, or EPCM/consultancy environments.
• Familiarity with GMP/GxP environments.
• Exposure to automation or digitally integrated manufacturing environments.

Responsabilités

• Develop and review process designs, PFDs, P&IDs, technical specifications etc.
• Support process development and scale-up activities for pharmaceutical manufacturing systems.
• Collaborate with automation engineers on process control strategies.
• Participate in FAT, SAT, commissioning, and qualification activities.
• Perform process calculations, risk assessments, and optimisation studies.
• Ensure compliance with GMP and regulatory requirements.
• Support troubleshooting and continuous improvement initiatives.
• Contribute to validation and technical documentation.

Connaissances

Process engineering

GMP / GxP awareness

Client & stakeholder engagement

Cross-functional teamwork

Analytical problem-solving

Formation

Bachelors in Chemical/Process Engineering or related

Outils

Emerson DeltaV

Siemens PCS7

Rockwell PlantPAx

Automation systems integration

Description du poste

ENGAGE GROUP PTE. LTD. in Singapore is seeking a Senior Process Engineer to lead process design in pharmaceutical and biotech manufacturing, bridging process engineering with automation to deliver GMP-compliant facilities.

You will work across concept through commissioning, collaborating with multidisciplinary teams, and applying knowledge of industry standards to optimise validation and CQV activities.